United States · FDA National Drug Code directory
Ultra Strength
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 21130-310_424a08be-ec47-a368-e063-6394a90a7e5b
- Product NDC
- 21130-310
- Form
- TABLET, CHEWABLE
- Composition / generic term
- Calcium Carbonate
- Labeler
- BETTER LIVING BRANDS LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200930
- Source listing expiry
- 20261231
Source-listed ingredients
- CALCIUM CARBONATE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 160 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (21130-310-60) · 21130-310-60
- 72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (21130-310-72) · 21130-310-72
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →